Vaterite: Difference between revisions
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'''Vaterite''' ([[calcium|Ca]][[carbon|C]][[oxygen|O]]<sub>3</sub>) is a mineral, a [[polymorphism (materials science)|polymorph]] of [[calcium carbonate]]. It was named after the German mineralogist [[Heinrich Vater]]. It is also known as mu-calcium carbonate ( |
'''Vaterite''' ([[calcium|Ca]][[carbon|C]][[oxygen|O]]<sub>3</sub>) is a mineral, a [[polymorphism (materials science)|polymorph]] of [[calcium carbonate]]. It was named after the German mineralogist [[Heinrich Vater]]. It is also known as mu-calcium carbonate (μ-CaCO<sub>3</sub>) and has a [[JCPDS]] number of 13-192. Vaterite, like aragonite, is a metastable phase of calcium carbonate at ambient conditions at the surface of the earth. As it is less stable than either calcite or aragonite, vaterite has a higher [[solubility]] than either of these phases. Therefore, once vaterite is exposed to [[water]], it converts to [[calcite]] (at low temperature) or [[aragonite]] (at high temperature: ~60 °C). However, vaterite does occur naturally in [[mineral spring]]s, organic tissue, [[gallstone]]s, and urinary calculi. In those circumstances, some impurities ([[metal]] ions or organic matter) may stabilize the vaterite and prevent its transformation into calcite or aragonite. Vaterite is usually colorless, its shape is spherical, and its diameter is small, ranging from 0.05 to 5 μm. |
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Vaterite can be produced as the first mineral deposits repairing natural or experimentally induced shell damage in some aragonite-shelled mollusks (e.g. gastropods). Subsequent shell deposition occurs as aragonite. |
Vaterite can be produced as the first mineral deposits repairing natural or experimentally induced shell damage in some aragonite-shelled mollusks (e.g. gastropods). Subsequent shell deposition occurs as aragonite. |
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[[Category:Carbonate minerals]] |
[[Category:Carbonate minerals]] |
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[[Category:Hexagonal minerals]] |
[[Category:Hexagonal minerals]] |
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{{Carbonate-mineral-stub}} |
Revision as of 20:49, 12 December 2013
Vaterite | |
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General | |
Category | Carbonate minerals |
Formula (repeating unit) | CaCO3 |
Strunz classification | 05.AB.20 |
Crystal system | Hexagonal |
Space group | Hexagonal dihexagonal dipyramidal H-M symbol: 6/mmm (6/m 2/m 2/m) Space group: P63/mmc {P63/m 2/m 2/c} |
Unit cell | a = 4.13 Å, c = 8.49 Å; Z = 6 |
Identification | |
Color | Colorless |
Crystal habit | Fine fibrous crystals, typically less than 0.1 mm, in spherulitic aggregates. |
Fracture | Irregular to uneven, splintery |
Tenacity | Brittle |
Mohs scale hardness | 3 |
Luster | Sub-vitreous, waxy |
Diaphaneity | Transparent to semi-transparent |
Specific gravity | 2.54 |
Optical properties | Uniaxial (+) |
Refractive index | nω = 1.550 nε = 1.650 |
Birefringence | δ = 0.100 |
References | [1][2][3] |
Vaterite (CaCO3) is a mineral, a polymorph of calcium carbonate. It was named after the German mineralogist Heinrich Vater. It is also known as mu-calcium carbonate (μ-CaCO3) and has a JCPDS number of 13-192. Vaterite, like aragonite, is a metastable phase of calcium carbonate at ambient conditions at the surface of the earth. As it is less stable than either calcite or aragonite, vaterite has a higher solubility than either of these phases. Therefore, once vaterite is exposed to water, it converts to calcite (at low temperature) or aragonite (at high temperature: ~60 °C). However, vaterite does occur naturally in mineral springs, organic tissue, gallstones, and urinary calculi. In those circumstances, some impurities (metal ions or organic matter) may stabilize the vaterite and prevent its transformation into calcite or aragonite. Vaterite is usually colorless, its shape is spherical, and its diameter is small, ranging from 0.05 to 5 μm.
Vaterite can be produced as the first mineral deposits repairing natural or experimentally induced shell damage in some aragonite-shelled mollusks (e.g. gastropods). Subsequent shell deposition occurs as aragonite.
Vaterite belongs to the hexagonal crystal system, whereas calcite is trigonal and aragonite is orthorhombic.